Serum Carnosinase-1 and Albuminuria Rather than the CNDP1 Genotype Correlate with Urinary Carnosinase-1 in Diabetic and Nondiabetic Patients with Chronic Kidney Disease. (26th December 2019)

• Record Type: Journal Article
• Authors: Rodriguez-Niño, Angelica; Hauske, Sibylle J.; Herold, Anna; Qiu, Jiedong; van den Born, Jacob; Bakker, Stephan J. L.; Krämer, Bernhard K.; Yard, Benito A.
• Other Names: Geraldes Pedro M. Academic Editor.
• Is Part Of: Journal of diabetes research. Volume 2019(2019)
• Publication Date: 2019-12-26
• Subjects: Diabetes -- Periodicals; Diabetes -- Pathophysiology -- Periodicals; Diabetes -- Prevention -- Periodicals; Diabetes -- Etiology -- Periodicals; Diabetes -- Epidemiology -- Periodicals; Diabetes -- Pathogenesis -- Periodicals; 616.462005
• DOI: 10.1155/2019/6850628
• Languages: English
• ISSNs: 2314-6745

Abstract

Abstract : Background . Carnosinase-1 (CN-1) can be detected in 24 h urine of healthy individuals and patients with type 2 diabetes (T2DM). We aimed to assess whether urinary CN-1 is also reliably measured in spot urine and investigated its association with renal function and the albumin/creatinine ratio (ACR). We also assessed associations between the CNDP1 (CTG) n genotype and CN-1 concentrations in serum and urine. Methods . Patients with T2DM (n = 85 ) and nondiabetic patients with chronic kidney disease (CKD) (n = 26 ) stratified by albuminuria (ACR ≤ 300 mg / g or ACR > 300 mg / g ) recruited from the nephrology clinic and healthy subjects (n = 24 ) were studied. Results . Urinary CN-1 was more frequently detected and displayed higher concentrations in patients with ACR > 300 mg / g as compared to those with ACR ≤ 300 mg / g irrespective of the baseline disease (T2DM: 554 ng/ml [IQR 212-934 ng/ml] vs. 31 ng/ml [IQR 31-63 ng/ml] (p < 0.0001 ) and nondiabetic CKD: 197 ng/ml [IQR 112-739] vs. 31 ng/ml [IQR 31-226 ng/ml] (p = 0.015 )). A positive correlation between urinary CN-1 and ACR was found (r = 0.68, p < 0.0001 ). Multivariate linear regression analysis revealed that ACR and serum CN-1 concentrations but not eGFR or the CNDP1 genotype are independent predictors of urinary CN-1, explaining 47% of variation of urinary CN-1 concentrations (R 2 = 0.47, p < 0.0001 ). Conclusion . These results confirm and extend previous findings on urinary CN-1 concentrations, suggesting that assessment of CN-1 in spot urine is as reliable as in 24 h urine and may indicate that urinary CN-1 in macroalbuminuric patients is primarily serum-derived and not locally produced.